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ES2175329T3 - DOUBLE METAL CYANIDE CATALYSTS AND PROCEDURE FOR PRODUCERS. - Google Patents

DOUBLE METAL CYANIDE CATALYSTS AND PROCEDURE FOR PRODUCERS.

Info

Publication number
ES2175329T3
ES2175329T3 ES97901051T ES97901051T ES2175329T3 ES 2175329 T3 ES2175329 T3 ES 2175329T3 ES 97901051 T ES97901051 T ES 97901051T ES 97901051 T ES97901051 T ES 97901051T ES 2175329 T3 ES2175329 T3 ES 2175329T3
Authority
ES
Spain
Prior art keywords
dmc
catalysts
size
paste
bimethalian
Prior art date
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Expired - Lifetime
Application number
ES97901051T
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Spanish (es)
Inventor
Paul Bowman
Harry Hinney
Robert Meeker
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Bayer Antwerpen NV
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Bayer Antwerpen NV
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Application filed by Bayer Antwerpen NV filed Critical Bayer Antwerpen NV
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Publication of ES2175329T3 publication Critical patent/ES2175329T3/en
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Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00—Polymeric products of isocyanates or isothiocyanates
    • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40—High-molecular-weight compounds
    • C08G18/48—Polyethers
    • C08G18/4866—Polyethers having a low unsaturation value
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J27/00—Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • B01J27/24—Nitrogen compounds
    • B01J27/26—Cyanides
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0234—Nitrogen-, phosphorus-, arsenic- or antimony-containing compounds
    • B01J31/0255—Phosphorus containing compounds
    • B01J31/0267—Phosphines or phosphonium compounds, i.e. phosphorus bonded to at least one carbon atom, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, the other atoms bonded to phosphorus being either carbon or hydrogen
    • B01J31/0268—Phosphonium compounds, i.e. phosphine with an additional hydrogen or carbon atom bonded to phosphorous so as to result in a formal positive charge on phosphorous
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/04—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing carboxylic acids or their salts
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/20—Carbonyls
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/22—Organic complexes
    • B01J31/2204—Organic complexes the ligands containing oxygen or sulfur as complexing atoms
    • B01J31/2208—Oxygen, e.g. acetylacetonates
    • B01J31/2226—Anionic ligands, i.e. the overall ligand carries at least one formal negative charge
    • B01J31/223—At least two oxygen atoms present in one at least bidentate or bridging ligand
    • B01J31/2234—Beta-dicarbonyl ligands, e.g. acetylacetonates
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/26—Catalysts comprising hydrides, coordination complexes or organic compounds containing in addition, inorganic metal compounds not provided for in groups B01J31/02 - B01J31/24
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/40—Regeneration or reactivation
    • B01J31/4015—Regeneration or reactivation of catalysts containing metals
    • B01J31/4023—Regeneration or reactivation of catalysts containing metals containing iron group metals, noble metals or copper
    • B01J31/4038—Regeneration or reactivation of catalysts containing metals containing iron group metals, noble metals or copper containing noble metals
    • B01J31/4046—Regeneration or reactivation of catalysts containing metals containing iron group metals, noble metals or copper containing noble metals containing rhodium
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/132—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
    • C07C29/136—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
    • C07C29/14—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of a —CHO group
    • C07C29/141—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of a —CHO group with hydrogen or hydrogen-containing gases
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/16—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by oxo-reaction combined with reduction
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/56—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds
    • C07C45/57—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds with oxygen as the only heteroatom
    • C07C45/58—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds with oxygen as the only heteroatom in three-membered rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/78—Separation; Purification; Stabilisation; Use of additives
    • C07C45/80—Separation; Purification; Stabilisation; Use of additives by liquid-liquid treatment
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
    • C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
    • C08G65/26—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
    • C08G65/2642—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds characterised by the catalyst used
    • C08G65/2645—Metals or compounds thereof, e.g. salts
    • C08G65/2663—Metal cyanide catalysts, i.e. DMC's
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G65/00—Treatment of hydrocarbon oils by two or more hydrotreatment processes only
    • C10G65/02—Treatment of hydrocarbon oils by two or more hydrotreatment processes only plural serial stages only
    • C10G65/10—Treatment of hydrocarbon oils by two or more hydrotreatment processes only plural serial stages only including only cracking steps
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G65/00—Treatment of hydrocarbon oils by two or more hydrotreatment processes only
    • C10G65/02—Treatment of hydrocarbon oils by two or more hydrotreatment processes only plural serial stages only
    • C10G65/12—Treatment of hydrocarbon oils by two or more hydrotreatment processes only plural serial stages only including cracking steps and other hydrotreatment steps
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/40—Substitution reactions at carbon centres, e.g. C-C or C-X, i.e. carbon-hetero atom, cross-coupling, C-H activation or ring-opening reactions
    • B01J2231/48—Ring-opening reactions
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/02—Compositional aspects of complexes used, e.g. polynuclearity
    • B01J2531/0202—Polynuclearity
    • B01J2531/0211—Metal clusters, i.e. complexes comprising 3 to about 1000 metal atoms with metal-metal bonds to provide one or more all-metal (M)n rings, e.g. Rh4(CO)12
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80—Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82—Metals of the platinum group
    • B01J2531/822—Rhodium
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80—Complexes comprising metals of Group VIII as the central metal
    • B01J2531/84—Metals of the iron group
    • B01J2531/845—Cobalt
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/584—Recycling of catalysts

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Toxicology (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • General Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Polyethers (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Catalysts (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Epoxy Resins (AREA)

Abstract

SE DESCRIBEN CATALIZADORES MEJORADOS DE CIANURO BIMETALICO (DMC) UTILES PARA SINTETIZAR POLIMEROS EPOXIDICOS. UN CATALIZADOR ES UNA PASTA DE UN COMPUESTO DE CIANURO BIMETALICO (DMC), UN AGENTE COMPLEJANTE ORGANICO, Y AGUA. LA PASTA CONSISTE EN AL MENOS EL 90 % EN PESO APROXIMADAMENTE DE PARTICULAS CON UN TAMAÑO DE PARTICULA DE ENTRE 0,1 A 10 MICRAS APROXIMADAMENTE MEDIDAS POR DISPERSION DE LA LUZ EN DISPERSIONES DE POLIETER - POLIOL DE LAS PARTICULAS DEL CATALIZADOR. LOS CATALIZADORES PREFERIDOS TIENEN UNA DISTRIBUCION BIMODAL DEL TAMAÑO DE LAS PARTICULAS. LA PASTA CATALITICA ES MAS ACTIVA Y MAS SENCILLA DE PREPARAR QUE LOS CATALIZADORES EN POLVO DE DMC. LOS POLIOLES HECHOS A PARTIR DE LA PASTA CATALITICA POSEEN INSATURACIONES MENORES, VISCOSIDADES MENORES, Y DISTRIBUCIONES MAS ESTRECHAS DEL PESO MOLECULAR, Y SON UTILES PARA FABRICAR UNA DIVERSIDAD DE PRODUCTOS DE POLIURETANO. TAMBIEN SE OBTIENEN MEJORES RESULTADOS CON CATALIZADORES DMC EN FORMA DE POLVO DE UN TAMAÑO MUY PEQUEÑO DE PARTICULA.IMPROVED CATALYSTS OF BIMETHALIAN CYANIDE (DMC) USED TO SYNTHEIZE EPOXIDIC POLYMERS ARE DESCRIBED. A CATALYST IS A PASTE OF A BIMETHALIAN CYANIDE COMPOUND (DMC), AN ORGANIC COMPLEXING AGENT, AND WATER. THE PASTA CONSISTS OF AT LEAST 90% IN APPROXIMATELY WEIGHT OF PARTICLES WITH A SIZE OF PARTICULAR BETWEEN 0.1 TO 10 MICRONS APPROXIMATELY MEASURED BY DISPERSION OF LIGHT IN POLYETER DISPERSIONS - POLYOL PARTICLE DISPERSIONS. THE PREFERRED CATALYSTS HAVE A BIMODAL DISTRIBUTION OF THE SIZE OF THE PARTICLES. THE CATALYTIC PASTE IS MORE ACTIVE AND SIMPLE TO PREPARE THAN DMC POWDER CATALYSTS. THE POLIOLS MADE FROM THE CATALYTIC PASTE HAVE LOWER INSATURATIONS, MINOR VISCOSITIES, AND MORE STRANGE DISTRIBUTIONS OF THE MOLECULAR WEIGHT, AND ARE USEFUL TO MANUFACTURE A DIVERSITY OF POLYURETHANE PRODUCTS. BETTER RESULTS ARE ALSO OBTAINED WITH DMC CATALYSTS IN THE FORM OF POWDER OF A VERY SMALL SIZE OF PARTICLE.

ES97901051T 1996-01-19 1997-01-17 DOUBLE METAL CYANIDE CATALYSTS AND PROCEDURE FOR PRODUCERS. Expired - Lifetime ES2175329T3 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US08/588,751 US5639705A (en) 1996-01-19 1996-01-19 Double metal cyanide catalysts and methods for making them

Publications (1)

Publication Number Publication Date
ES2175329T3 true ES2175329T3 (en) 2002-11-16

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ID=24355145

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Application Number Title Priority Date Filing Date
ES97901051T Expired - Lifetime ES2175329T3 (en) 1996-01-19 1997-01-17 DOUBLE METAL CYANIDE CATALYSTS AND PROCEDURE FOR PRODUCERS.

Country Status (17)

Country Link
US (2) US5639705A (en)
EP (1) EP0877651B1 (en)
JP (1) JP2000513647A (en)
KR (1) KR100442702B1 (en)
CN (1) CN1090058C (en)
AR (1) AR005486A1 (en)
AU (1) AU709419B2 (en)
BR (1) BR9707122A (en)
CA (1) CA2243068C (en)
CZ (1) CZ294262B6 (en)
DE (1) DE69712039T2 (en)
ES (1) ES2175329T3 (en)
ID (1) ID15915A (en)
MX (1) MX9805411A (en)
PL (1) PL327821A1 (en)
TW (1) TW394783B (en)
WO (1) WO1997026080A1 (en)

Families Citing this family (57)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5689012A (en) * 1996-07-18 1997-11-18 Arco Chemical Technology, L.P. Continuous preparation of low unsaturation polyoxyalkylene polyether polyols with continuous additon of starter
US5693584A (en) * 1996-08-09 1997-12-02 Arco Chemical Technology, L.P. Highly active double metal cyanide catalysts
DE19709031A1 (en) * 1997-03-06 1998-09-10 Basf Ag Process for the preparation of double metal cyanide catalysts
US5891818A (en) * 1997-07-31 1999-04-06 Arco Chemical Technology, L.P. Cyanide complex catalyst manufacturing process
US6624286B2 (en) 1997-10-13 2003-09-23 Bayer Aktiengesellschaft Double-metal cyanide catalysts containing polyester for preparing polyether polyols
CN1273217C (en) 1997-10-13 2006-09-06 拜尔公司 Double metal cyanide catalysts containing polyester for preparing polyether polyoles `
AR019107A1 (en) * 1998-04-27 2001-12-26 Dow Global Technologies Inc HIGH MOLECULAR WEIGHT POLIOLS, PROCESS FOR THEIR PREPARATION AND USE OF THE SAME.
US6051680A (en) * 1998-06-08 2000-04-18 Arco Chemical Technology, L.P. Silylated double metal cyanide complex catalysts
DE19840585A1 (en) † 1998-09-05 2000-03-09 Basf Ag Process for the preparation of polyetherols by ring-opening polymerization of alkylene oxides
US6800583B2 (en) * 1999-06-02 2004-10-05 Basf Aktiengesellschaft Suspension of multimetal cyanide compounds, their preparation and their use
US7169889B1 (en) * 1999-06-19 2007-01-30 Biocon Limited Insulin prodrugs hydrolyzable in vivo to yield peglylated insulin
US20040266982A1 (en) * 1999-07-09 2004-12-30 Clement Katherine S Polymerization of alkylene oxides onto functionalized initiators
AU2001255735A1 (en) 2000-04-28 2001-11-12 Synuthane International, Inc. Double metal cyanide catalysts containing polyglycol ether complexing agents
US6429166B1 (en) 2000-05-19 2002-08-06 Dow Global Technologies Inc. Method for preparing metal cyanide catalyst/polyol initiator slurries
US6348565B1 (en) 2000-05-19 2002-02-19 The Dow Chemical Company Method for preparing metal cyanide catalysts using silane-functional ligands
AR024683A1 (en) * 2000-05-19 2002-10-23 Dow Chemical Co METHOD TO PREPARE METAL CYANIDE CATALYSTS AND TO USE THEM.
US6436867B1 (en) 2000-08-01 2002-08-20 Basf Corporation One-step synthesis of double metal cyanides
WO2002051428A1 (en) * 2000-12-25 2002-07-04 Shiseido Company, Ltd. Sympathetic-activating perfume composition
US6867183B2 (en) * 2001-02-15 2005-03-15 Nobex Corporation Pharmaceutical compositions of insulin drug-oligomer conjugates and methods of treating diseases therewith
US6713452B2 (en) 2001-06-04 2004-03-30 Nobex Corporation Mixtures of calcitonin drug-oligomer conjugates comprising polyalkylene glycol, uses thereof, and methods of making same
US7713932B2 (en) * 2001-06-04 2010-05-11 Biocon Limited Calcitonin drug-oligomer conjugates, and uses thereof
US6835802B2 (en) 2001-06-04 2004-12-28 Nobex Corporation Methods of synthesizing substantially monodispersed mixtures of polymers having polyethylene glycol moieties
US6828297B2 (en) * 2001-06-04 2004-12-07 Nobex Corporation Mixtures of insulin drug-oligomer conjugates comprising polyalkylene glycol, uses thereof, and methods of making same
US6828305B2 (en) * 2001-06-04 2004-12-07 Nobex Corporation Mixtures of growth hormone drug-oligomer conjugates comprising polyalkylene glycol, uses thereof, and methods of making same
US6858580B2 (en) 2001-06-04 2005-02-22 Nobex Corporation Mixtures of drug-oligomer conjugates comprising polyalkylene glycol, uses thereof, and methods of making same
DE10141122A1 (en) * 2001-08-22 2003-03-13 Basf Ag Process for increasing the catalytic activity of multimetal cyanide compounds
EP1288244A1 (en) * 2001-08-31 2003-03-05 Asahi Glass Company, Limited Double metal cyanide complex catalyst for ring opening polymerization of alkylene oxide and its production process
US7196059B2 (en) * 2001-09-07 2007-03-27 Biocon Limited Pharmaceutical compositions of insulin drug-oligomer conjugates and methods of treating diseases therewith
US6541673B1 (en) 2001-11-30 2003-04-01 Arco Chemical Technology, L.P. Process for oxyalkylating phenolic compounds
DE10205086A1 (en) † 2002-02-07 2003-08-21 Basf Ag Process for the activation of double metal cyanide compounds
AU2003220309B2 (en) * 2002-03-19 2008-09-25 Dow Global Technologies, Inc. Method for preparing metal cyanide catalysts using insoluble metal salts
WO2003105768A2 (en) 2002-06-13 2003-12-24 Nobex Corporation Methods of reducing hypoglycemic episodes in the treatment of diabetes mellitus
US6835801B2 (en) * 2002-07-19 2004-12-28 Bayer Antwerp, N.V. Activated starter mixtures and the processes related thereto
US7001634B2 (en) * 2002-11-07 2006-02-21 Bayer Materialscience Llc Process for suppressing the foaming of an aqueous system
ZA200503601B (en) * 2002-11-07 2006-11-29 Dow Global Technologies Inc Method for preparing metal cyanide catalysts using polymerizable complexing agents
CA2526619C (en) * 2003-05-22 2011-09-13 Dow Global Technologies Inc. Nano-scale dmc catalyst particles
WO2004108794A1 (en) * 2003-06-04 2004-12-16 Asahi Glass Company, Limited Composite metal cyanide complex catalyst, process for producing the same, and use of the same
JP4556496B2 (en) * 2003-06-04 2010-10-06 旭硝子株式会社 Double metal cyanide complex catalyst, production method thereof and use thereof
US7223890B2 (en) * 2003-10-10 2007-05-29 Bayer Materialscience Llc Isocyanate reactive mixture and process for preparing same
US20060182692A1 (en) 2003-12-16 2006-08-17 Fishburn C S Chemically modified small molecules
EA015333B1 (en) * 2003-12-16 2011-06-30 Нектар Терапьютикс Compositions comprising conjugates, methods for producing thereof and use
US6869905B1 (en) 2004-03-02 2005-03-22 Basf Corporation Synthesis of double metal cyanides with non-aqueous solutions
US20060058182A1 (en) * 2004-09-13 2006-03-16 Combs George G Processes for the preparation of double metal cyanide (DMC) catalysts
KR101315527B1 (en) * 2004-10-26 2013-10-08 다우 글로벌 테크놀로지스 엘엘씨 Improved method for alkoxylating active hydrogen containing compounds and the alkoxylated compounds made therefrom
EP1861199A1 (en) * 2005-03-22 2007-12-05 Shell Internationale Research Maatschappij B.V. Process for the preparation of an improved double metal cyanide complex catalyst, double metal cyanide catalyst and use of such catalyst
JP5251510B2 (en) * 2006-08-31 2013-07-31 旭硝子株式会社 Method for purifying polyethers
CN101516954B (en) 2006-09-27 2011-07-20 旭硝子株式会社 Method for producing soft polyurethane foam
KR20120088690A (en) 2009-09-30 2012-08-08 아사히 가라스 가부시키가이샤 Method for manufacturing an isocyanate-terminated prepolymer, prepolymer obtained thereby, and polyurethane resin
WO2011043345A1 (en) 2009-10-05 2011-04-14 旭硝子株式会社 Soft polyurethane foam, method for producing the same, and seat cushion for automobile
WO2011047780A1 (en) 2009-10-19 2011-04-28 Basf Se Conditioning of double metal cyanide catalysts
WO2011136367A1 (en) 2010-04-30 2011-11-03 旭硝子株式会社 Polyoxyalkylene polyol, polyol in which polymer is dispersed, flexible polyurethane foam, and processes for production of same
WO2011160296A1 (en) 2010-06-23 2011-12-29 Basf Se Modified double metal cyanide catalyst
CN102274740B (en) * 2011-06-17 2013-02-06 浙江大学 A method for preparing metal cyanide nanoparticles
US9139691B2 (en) 2011-06-30 2015-09-22 Bayer Intellectual Property Gmbh Process for preparing high molecular weight polyether polyols
WO2013028437A1 (en) 2011-08-25 2013-02-28 Dow Global Technologies Llc Process for making polyether alcohols having oxyethylene units by polymerization of ethylene carbonate in the presence of double metal cyanide catalysts
CN112126053B (en) * 2020-09-22 2022-06-21 河北工业大学 Preparation method and application of double metal cyanide catalyst
PL442356A1 (en) 2022-09-26 2024-04-02 Pcc Rokita Spółka Akcyjna Polyether polyol, its production method and its use, and flexible polyurethane foam

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3278458A (en) * 1963-02-14 1966-10-11 Gen Tire & Rubber Co Method of making a polyether using a double metal cyanide complex compound
US3278457A (en) * 1963-02-14 1966-10-11 Gen Tire & Rubber Co Method of making a polyether using a double metal cyanide complex compound
DE1770548A1 (en) * 1967-06-02 1972-02-10 Gen Tire & Rubber Co Polyester and its manufacture
US3900518A (en) * 1967-10-20 1975-08-19 Gen Tire & Rubber Co Hydroxyl or thiol terminated telomeric ethers
US3829505A (en) * 1970-02-24 1974-08-13 Gen Tire & Rubber Co Polyethers and method for making the same
US3941849A (en) * 1972-07-07 1976-03-02 The General Tire & Rubber Company Polyethers and method for making the same
AU551979B2 (en) * 1982-03-31 1986-05-15 Shell Internationale Research Maatschappij B.V. Epoxy polymerisation catalysts
AU552988B2 (en) * 1982-03-31 1986-06-26 Shell Internationale Research Maatschappij B.V. Polymerizing epoxides and catalyst suspensions for this
JP2995568B2 (en) * 1989-05-09 1999-12-27 旭硝子株式会社 Manufacture of polyalkylene oxide derivative
JP3097854B2 (en) * 1989-05-12 2000-10-10 旭硝子株式会社 Method for producing polyurethanes
JP2653236B2 (en) * 1990-10-05 1997-09-17 旭硝子株式会社 Method for producing polyether compound
US5158922A (en) * 1992-02-04 1992-10-27 Arco Chemical Technology, L.P. Process for preparing metal cyanide complex catalyst
US5470813A (en) * 1993-11-23 1995-11-28 Arco Chemical Technology, L.P. Double metal cyanide complex catalysts

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